| Name | Number of Publications
|
Most Recent Publication
|
Publications by All Authors
|
Concept Score
|
Why?
|
|---|
| Mitochondrial Diseases | 7 | 2018 | 344 | 0.900 |
Why?
|
| Plasma Membrane Neurotransmitter Transport Proteins | 5 | 2020 | 23 | 0.640 |
Why?
|
| Lissencephaly | 1 | 2016 | 36 | 0.540 |
Why?
|
| Cytochrome Reductases | 1 | 2015 | 9 | 0.500 |
Why?
|
| Atrophy | 1 | 2020 | 1646 | 0.470 |
Why?
|
| Peptide Termination Factors | 1 | 2014 | 56 | 0.450 |
Why?
|
| Acidosis, Lactic | 1 | 2015 | 145 | 0.440 |
Why?
|
| Optic Atrophy | 1 | 2014 | 79 | 0.430 |
Why?
|
| Adrenal Insufficiency | 1 | 2015 | 195 | 0.420 |
Why?
|
| Leigh Disease | 1 | 2014 | 89 | 0.420 |
Why?
|
| Tubulin | 1 | 2016 | 695 | 0.420 |
Why?
|
| Angelman Syndrome | 4 | 2019 | 139 | 0.380 |
Why?
|
| Siblings | 2 | 2016 | 828 | 0.360 |
Why?
|
| Dystonic Disorders | 2 | 2016 | 354 | 0.330 |
Why?
|
| Genetic Predisposition to Disease | 6 | 2021 | 18065 | 0.330 |
Why?
|
| Genetic Variation | 5 | 2021 | 6611 | 0.330 |
Why?
|
| Aromatic-L-Amino-Acid Decarboxylases | 2 | 2021 | 27 | 0.320 |
Why?
|
| Cataract | 1 | 2015 | 837 | 0.320 |
Why?
|
| Nerve Tissue Proteins | 5 | 2017 | 4413 | 0.300 |
Why?
|
| Ventricular Premature Complexes | 1 | 2008 | 112 | 0.280 |
Why?
|
| Phenotype | 14 | 2021 | 16726 | 0.280 |
Why?
|
| Sodium-Potassium-Exchanging ATPase | 1 | 2009 | 480 | 0.270 |
Why?
|
| Parkinsonian Disorders | 1 | 2009 | 285 | 0.260 |
Why?
|
| MELAS Syndrome | 1 | 2006 | 55 | 0.260 |
Why?
|
| Frameshift Mutation | 1 | 2008 | 392 | 0.260 |
Why?
|
| Betaine | 2 | 2019 | 90 | 0.250 |
Why?
|
| Mental Retardation, X-Linked | 4 | 2020 | 42 | 0.250 |
Why?
|
| Mutation | 9 | 2021 | 30238 | 0.250 |
Why?
|
| Muscle Hypotonia | 2 | 2020 | 166 | 0.230 |
Why?
|
| Chromosomes, Human, X | 1 | 2006 | 320 | 0.220 |
Why?
|
| Norepinephrine | 1 | 2006 | 898 | 0.220 |
Why?
|
| Metabolism, Inborn Errors | 1 | 2006 | 292 | 0.220 |
Why?
|
| Creatine | 4 | 2020 | 427 | 0.220 |
Why?
|
| Cardiotonic Agents | 1 | 2006 | 542 | 0.210 |
Why?
|
| Vasoconstrictor Agents | 1 | 2006 | 656 | 0.200 |
Why?
|
| Carboxy-Lyases | 1 | 2021 | 85 | 0.190 |
Why?
|
| Heterogeneous-Nuclear Ribonucleoproteins | 1 | 2021 | 69 | 0.180 |
Why?
|
| Brain Diseases, Metabolic, Inborn | 3 | 2020 | 46 | 0.180 |
Why?
|
| Peripheral Nervous System Diseases | 1 | 2006 | 716 | 0.180 |
Why?
|
| Epilepsy | 4 | 2020 | 3327 | 0.180 |
Why?
|
| Membrane Transport Proteins | 1 | 2006 | 1037 | 0.170 |
Why?
|
| DNA | 1 | 2014 | 7214 | 0.170 |
Why?
|
| Chromosomes, Human, Pair 15 | 3 | 2011 | 361 | 0.170 |
Why?
|
| Developmental Disabilities | 1 | 2008 | 1518 | 0.160 |
Why?
|
| Dopamine | 1 | 2006 | 1592 | 0.160 |
Why?
|
| GTP-Binding Protein alpha Subunits, Gi-Go | 1 | 2019 | 89 | 0.160 |
Why?
|
| Folic Acid | 2 | 2019 | 1337 | 0.160 |
Why?
|
| Carbon-Nitrogen Ligases | 1 | 2018 | 27 | 0.150 |
Why?
|
| Amino Acid Transport Systems, Acidic | 1 | 2018 | 30 | 0.150 |
Why?
|
| Acyltransferases | 1 | 2020 | 306 | 0.150 |
Why?
|
| Hereditary Central Nervous System Demyelinating Diseases | 1 | 2018 | 44 | 0.150 |
Why?
|
| Cerebellar Diseases | 1 | 2020 | 227 | 0.150 |
Why?
|
| Microcephaly | 2 | 2020 | 426 | 0.150 |
Why?
|
| Craniofacial Abnormalities | 1 | 2020 | 320 | 0.150 |
Why?
|
| Psychomotor Disorders | 1 | 2018 | 149 | 0.140 |
Why?
|
| Succinate-CoA Ligases | 1 | 2016 | 6 | 0.140 |
Why?
|
| Genetic Association Studies | 4 | 2021 | 2744 | 0.140 |
Why?
|
| Apoptosis Inducing Factor | 1 | 2017 | 51 | 0.140 |
Why?
|
| Mitochondrial Encephalomyopathies | 1 | 2017 | 40 | 0.140 |
Why?
|
| Antiporters | 1 | 2018 | 276 | 0.140 |
Why?
|
| Arrhythmias, Cardiac | 1 | 2006 | 2258 | 0.130 |
Why?
|
| Heterozygote | 2 | 2020 | 2798 | 0.130 |
Why?
|
| Charcot-Marie-Tooth Disease | 1 | 2017 | 102 | 0.130 |
Why?
|
| Adenosine Triphosphatases | 1 | 2020 | 842 | 0.130 |
Why?
|
| Hyperkinesis | 1 | 2016 | 88 | 0.130 |
Why?
|
| Morocco | 1 | 2015 | 36 | 0.130 |
Why?
|
| Oxidoreductases Acting on Sulfur Group Donors | 1 | 2015 | 32 | 0.130 |
Why?
|
| Chorea | 1 | 2016 | 80 | 0.120 |
Why?
|
| Growth Disorders | 1 | 2020 | 635 | 0.120 |
Why?
|
| Child, Preschool | 12 | 2020 | 42669 | 0.110 |
Why?
|
| Child | 19 | 2020 | 80917 | 0.110 |
Why?
|
| Cholestasis, Intrahepatic | 1 | 2014 | 75 | 0.110 |
Why?
|
| Sequence Deletion | 3 | 2019 | 1497 | 0.110 |
Why?
|
| Cell Adhesion Molecules | 1 | 2020 | 1613 | 0.110 |
Why?
|
| Microfilament Proteins | 1 | 2018 | 1133 | 0.110 |
Why?
|
| DNA Mutational Analysis | 2 | 2014 | 4120 | 0.110 |
Why?
|
| Consanguinity | 1 | 2015 | 460 | 0.110 |
Why?
|
| Chromosome Aberrations | 2 | 2011 | 1778 | 0.110 |
Why?
|
| Standard of Care | 1 | 2017 | 568 | 0.100 |
Why?
|
| Psychometrics | 2 | 2020 | 3063 | 0.100 |
Why?
|
| Brain Diseases, Metabolic | 1 | 2012 | 44 | 0.100 |
Why?
|
| Rhabdomyolysis | 1 | 2012 | 150 | 0.090 |
Why?
|
| ATP-Binding Cassette Transporters | 1 | 2014 | 567 | 0.090 |
Why?
|
| Neuropsychological Tests | 2 | 2020 | 7140 | 0.090 |
Why?
|
| Amino Acid Metabolism, Inborn Errors | 1 | 2012 | 283 | 0.080 |
Why?
|
| Brain | 7 | 2021 | 27360 | 0.080 |
Why?
|
| Dystonia | 1 | 2012 | 378 | 0.080 |
Why?
|
| Humans | 34 | 2021 | 768166 | 0.080 |
Why?
|
| Mitochondrial Proteins | 1 | 2014 | 979 | 0.070 |
Why?
|
| Fatal Outcome | 2 | 2016 | 1836 | 0.070 |
Why?
|
| Male | 22 | 2020 | 364719 | 0.070 |
Why?
|
| Deep Brain Stimulation | 1 | 2016 | 851 | 0.070 |
Why?
|
| Parkinson Disease | 1 | 2021 | 2893 | 0.070 |
Why?
|
| Nervous System Malformations | 2 | 2020 | 243 | 0.070 |
Why?
|
| Magnetic Resonance Spectroscopy | 2 | 2008 | 3780 | 0.070 |
Why?
|
| Language Development Disorders | 1 | 2008 | 194 | 0.070 |
Why?
|
| Sural Nerve | 1 | 2006 | 105 | 0.070 |
Why?
|
| Peroneal Nerve | 1 | 2006 | 80 | 0.070 |
Why?
|
| Carrier Proteins | 1 | 2018 | 4937 | 0.060 |
Why?
|
| Electrocardiography, Ambulatory | 1 | 2008 | 582 | 0.060 |
Why?
|
| Mitochondria | 2 | 2017 | 3681 | 0.060 |
Why?
|
| Neural Conduction | 1 | 2006 | 443 | 0.060 |
Why?
|
| Infant | 9 | 2020 | 36535 | 0.060 |
Why?
|
| Amino Acid Substitution | 1 | 2009 | 1743 | 0.060 |
Why?
|
| Muscle, Skeletal | 2 | 2017 | 4978 | 0.060 |
Why?
|
| Glycine | 1 | 2008 | 672 | 0.060 |
Why?
|
| Brain Chemistry | 1 | 2008 | 958 | 0.060 |
Why?
|
| Ubiquitin-Protein Ligases | 2 | 2011 | 1901 | 0.060 |
Why?
|
| Vasculitis, Central Nervous System | 1 | 2004 | 45 | 0.060 |
Why?
|
| Family | 1 | 2015 | 3209 | 0.060 |
Why?
|
| Adolescent | 7 | 2020 | 89169 | 0.050 |
Why?
|
| Vitamin B Complex | 2 | 2019 | 299 | 0.050 |
Why?
|
| Gene Deletion | 2 | 2014 | 2675 | 0.050 |
Why?
|
| Deglutition Disorders | 1 | 2009 | 640 | 0.050 |
Why?
|
| Child Behavior Disorders | 1 | 2008 | 812 | 0.050 |
Why?
|
| Comparative Genomic Hybridization | 2 | 2018 | 474 | 0.050 |
Why?
|
| Genetic Markers | 1 | 2009 | 2603 | 0.050 |
Why?
|
| Age of Onset | 1 | 2009 | 3347 | 0.050 |
Why?
|
| Exons | 1 | 2008 | 2394 | 0.050 |
Why?
|
| Heart Arrest | 1 | 2012 | 1516 | 0.050 |
Why?
|
| Double-Blind Method | 3 | 2019 | 12465 | 0.050 |
Why?
|
| Eye | 1 | 2006 | 712 | 0.050 |
Why?
|
| Female | 13 | 2020 | 397192 | 0.050 |
Why?
|
| DNA, Mitochondrial | 2 | 2017 | 872 | 0.050 |
Why?
|
| Polymorphism, Single Nucleotide | 2 | 2018 | 16045 | 0.040 |
Why?
|
| Transcription Factors | 1 | 2020 | 12168 | 0.040 |
Why?
|
| Putamen | 1 | 2021 | 291 | 0.040 |
Why?
|
| DNA Methylation | 2 | 2011 | 4428 | 0.040 |
Why?
|
| Cross-Over Studies | 1 | 2006 | 2107 | 0.040 |
Why?
|
| Acute Kidney Injury | 1 | 2012 | 1942 | 0.040 |
Why?
|
| Action Potentials | 1 | 2006 | 1838 | 0.040 |
Why?
|
| Progeria | 1 | 2001 | 188 | 0.040 |
Why?
|
| Inheritance Patterns | 1 | 2021 | 344 | 0.040 |
Why?
|
| Autistic Disorder | 1 | 2008 | 1240 | 0.040 |
Why?
|
| Genotype | 2 | 2013 | 13045 | 0.040 |
Why?
|
| Acute Disease | 1 | 2009 | 7243 | 0.040 |
Why?
|
| RNA Processing, Post-Transcriptional | 1 | 2021 | 393 | 0.040 |
Why?
|
| Neuroaxonal Dystrophies | 1 | 2018 | 26 | 0.040 |
Why?
|
| Dietary Supplements | 1 | 2011 | 3445 | 0.040 |
Why?
|
| Folate Receptor 1 | 1 | 2018 | 41 | 0.040 |
Why?
|
| Tetrahydrofolates | 1 | 2018 | 58 | 0.040 |
Why?
|
| Facies | 1 | 2018 | 224 | 0.040 |
Why?
|
| Twins, Monozygotic | 1 | 2019 | 472 | 0.040 |
Why?
|
| Young Adult | 4 | 2020 | 60066 | 0.030 |
Why?
|
| Epilepsies, Partial | 1 | 2001 | 435 | 0.030 |
Why?
|
| Base Sequence | 1 | 2008 | 12421 | 0.030 |
Why?
|
| Membrane Proteins | 1 | 2014 | 7876 | 0.030 |
Why?
|
| Electron Transport | 1 | 2017 | 211 | 0.030 |
Why?
|
| Cerebral Infarction | 1 | 2001 | 969 | 0.030 |
Why?
|
| Genetic Diseases, Inborn | 1 | 2020 | 606 | 0.030 |
Why?
|
| Molecular Sequence Data | 1 | 2008 | 17622 | 0.030 |
Why?
|
| Physicians | 1 | 2013 | 4598 | 0.030 |
Why?
|
| Follow-Up Studies | 2 | 2014 | 39348 | 0.030 |
Why?
|
| Phosphorylation | 1 | 2006 | 8317 | 0.030 |
Why?
|
| Gastrointestinal Agents | 1 | 2019 | 511 | 0.030 |
Why?
|
| Oxygen | 1 | 2006 | 4270 | 0.030 |
Why?
|
| Syndrome | 1 | 2020 | 3272 | 0.030 |
Why?
|
| Carotid Stenosis | 1 | 2001 | 859 | 0.030 |
Why?
|
| Positron-Emission Tomography | 1 | 2009 | 6669 | 0.030 |
Why?
|
| Glutaryl-CoA Dehydrogenase | 1 | 2012 | 19 | 0.030 |
Why?
|
| Genes, X-Linked | 1 | 2013 | 129 | 0.030 |
Why?
|
| Abnormalities, Multiple | 1 | 2020 | 1424 | 0.030 |
Why?
|
| Muscular Diseases | 1 | 2017 | 553 | 0.030 |
Why?
|
| DNA Copy Number Variations | 1 | 2021 | 2048 | 0.020 |
Why?
|
| Pedigree | 1 | 2020 | 4539 | 0.020 |
Why?
|
| Disease Progression | 1 | 2009 | 13671 | 0.020 |
Why?
|
| Adrenoleukodystrophy | 1 | 2014 | 144 | 0.020 |
Why?
|
| Mutation, Missense | 1 | 2021 | 2592 | 0.020 |
Why?
|
| Metabolic Diseases | 1 | 2018 | 684 | 0.020 |
Why?
|
| Adult | 6 | 2020 | 223646 | 0.020 |
Why?
|
| Magnetic Resonance Imaging | 3 | 2017 | 36743 | 0.020 |
Why?
|
| Lipotropic Agents | 1 | 2010 | 13 | 0.020 |
Why?
|
| Delphi Technique | 1 | 2014 | 891 | 0.020 |
Why?
|
| Leukocytes | 1 | 2018 | 2035 | 0.020 |
Why?
|
| North America | 1 | 2013 | 1289 | 0.020 |
Why?
|
| Electroencephalography | 2 | 2018 | 6314 | 0.020 |
Why?
|
| Single-Cell Analysis | 1 | 2021 | 2540 | 0.020 |
Why?
|
| Randomized Controlled Trials as Topic | 1 | 2006 | 10399 | 0.020 |
Why?
|
| Alleles | 1 | 2020 | 6894 | 0.020 |
Why?
|
| Genomic Imprinting | 1 | 2010 | 326 | 0.020 |
Why?
|
| Fibroblasts | 1 | 2018 | 4176 | 0.020 |
Why?
|
| Gene Duplication | 1 | 2008 | 315 | 0.020 |
Why?
|
| Disease Management | 1 | 2017 | 2536 | 0.020 |
Why?
|
| Placebos | 1 | 2010 | 1667 | 0.020 |
Why?
|
| Statistics, Nonparametric | 1 | 2011 | 2862 | 0.020 |
Why?
|
| Immunohistochemistry | 1 | 2018 | 11095 | 0.020 |
Why?
|
| Consensus | 1 | 2014 | 3212 | 0.010 |
Why?
|
| Drug Combinations | 1 | 2010 | 2089 | 0.010 |
Why?
|
| Chromosome Deletion | 1 | 2008 | 1385 | 0.010 |
Why?
|
| Gene Expression Regulation | 1 | 2021 | 11928 | 0.010 |
Why?
|
| Evidence-Based Medicine | 1 | 2014 | 3706 | 0.010 |
Why?
|
| Data Collection | 1 | 2011 | 3327 | 0.010 |
Why?
|
| Case-Control Studies | 1 | 2019 | 22291 | 0.010 |
Why?
|
| Diffusion Magnetic Resonance Imaging | 1 | 2012 | 2815 | 0.010 |
Why?
|
| Genetic Testing | 1 | 2013 | 3591 | 0.010 |
Why?
|
| Intracranial Arteriosclerosis | 1 | 2001 | 138 | 0.010 |
Why?
|
| Middle Aged | 2 | 2020 | 223492 | 0.010 |
Why?
|
| Carotid Artery, Internal | 1 | 2001 | 440 | 0.010 |
Why?
|
| Treatment Outcome | 2 | 2014 | 65371 | 0.010 |
Why?
|
| Pregnancy | 1 | 2017 | 30256 | 0.010 |
Why?
|
| Longitudinal Studies | 1 | 2011 | 14783 | 0.010 |
Why?
|
| Magnetic Resonance Angiography | 1 | 2001 | 1429 | 0.010 |
Why?
|
| Infant, Newborn | 1 | 2014 | 26422 | 0.010 |
Why?
|
| Radiography | 1 | 2004 | 6983 | 0.010 |
Why?
|
| Retrospective Studies | 1 | 2013 | 81762 | 0.000 |
Why?
|